A spontaneous missense mutation in the chromodomain helicase DNA-binding protein 8 (CHD8) gene: a novel association with congenital myasthenic syndrome. [electronic resource]
Producer: 20211025Description: 588-601 p. digitalISSN:- 1365-2990
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Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't; Twin Study
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